BEUDAMED
    6 results · 21ms · Sources: EU EUDAMED, US FDA

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    ARGYLE NEO-SERT TRIPLE LUMEN UMBILICAL VESSEL CATHETER

    FDA 510(k)
    FDA Class 2 ·General Hospital

    Single Use Aspiration Needle NA-U200H

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    SECUR-FIT MAX AND PLUS MAX HIP STEMS

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    REVEAL XT

    FDA Adverse Event
    Injury ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code DSI·February 9, 2013

    SYSTEM, PERITONEAL, AUTOMATIC DELIVERY

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code FKX·July 23, 2014

    IMMAGE® 800 IMMUNOCHEMISTRY SYSTEM

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER, INC.·Product code JQX·January 6, 2011